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NM_014874.4(MFN2):c.624G>T (p.Glu208Asp) AND not provided

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Jun 21, 2019
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000761641.19

Allele description [Variation Report for NM_014874.4(MFN2):c.624G>T (p.Glu208Asp)]

NM_014874.4(MFN2):c.624G>T (p.Glu208Asp)

Gene:
MFN2:mitofusin 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p36.22
Genomic location:
Preferred name:
NM_014874.4(MFN2):c.624G>T (p.Glu208Asp)
HGVS:
  • NC_000001.11:g.11998794G>T
  • NG_007945.1:g.23614G>T
  • NM_001127660.2:c.624G>T
  • NM_014874.4:c.624G>TMANE SELECT
  • NP_001121132.1:p.Glu208Asp
  • NP_055689.1:p.Glu208Asp
  • NP_055689.1:p.Glu208Asp
  • LRG_255t1:c.624G>T
  • LRG_255:g.23614G>T
  • LRG_255p1:p.Glu208Asp
  • NC_000001.10:g.12058851G>T
  • NM_014874.3:c.624G>T
Protein change:
E208D
Links:
dbSNP: rs1162977959
NCBI 1000 Genomes Browser:
rs1162977959
Molecular consequence:
  • NM_001127660.2:c.624G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_014874.4:c.624G>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
3

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000891811CeGaT Center for Human Genetics Tuebingen
criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)		Uncertain significance
(Feb 1, 2019) 		germlineclinical testing

Citation Link,

SCV001992776GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Jun 21, 2019) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes3not providednot providednot providednot providedclinical testing

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV000891811.22

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided3not providednot providednot provided

From GeneDx, SCV001992776.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

Has not been previously published as pathogenic or benign to our knowledge; Not observed in large population cohorts (Lek et al., 2016); In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Apr 15, 2024